1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid

group of stereoisomers with the chemical formula C₁₄H₁₆O₁₀
ChemicalSubstance group_of_stereoisomers Q104393036
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1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid

Summary

1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid is a group of stereoisomers[1].

Key Facts

  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's instance of is recorded as group of stereoisomers[2].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's canonical SMILES is recorded as O=C(O)C1(O)CC(O)C(O)C(OC(=O)C2=CC(O)=C(O)C(O)=C2)C1[3].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's InChI is recorded as InChI=1S/C14H16O10/c15-6-1-5(2-7(16)10(6)18)12(20)24-9-4-14(23,13(21)22)3-8(17)11(9)19/h1-2,8-9,11,15-19,23H,3-4H2,(H,21,22)[4].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's InChIKey is recorded as LDPLFHGGZNSKDS-UHFFFAOYSA-N[5].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's chemical formula is recorded as C₁₄H₁₆O₁₀[6].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's subclass of is recorded as chemical compound[7].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's PubChem CID is recorded as 4486613[8].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's found in taxon is recorded as Quercus aliena[9].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's found in taxon is recorded as Eriogonum umbellatum[10].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's found in taxon is recorded as Cistus creticus[11].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's Human Metabolome Database ID is recorded as HMDB0039287[12].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+344.0743467119999'}[13].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's SureChEMBL ID is recorded as 17220945[14].
  • 1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid's UniChem compound ID is recorded as 32016789[15].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . PubChem. Retrieved . wikidata.org.
  8. [9] . Tannins and related compounds. CIX. Isolation of alienanins A and B, novel C,C-linked ellagitannin dimers from Quercus aliena Blume.. wikidata.org.
  9. [10] . Metabolites of Eriogonum umbellatum. wikidata.org.
  10. [11] . Phytochemical analysis of the labdanum-poor Cistus creticus subsp. eriocephalus (Viv.) Greuter et Burdet growing in central Italy. wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . UniChem. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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MLA “1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/1-3-4-trihydroxy-5-3-4-5-trihydroxybenzoyl-oxycyclohexane-1-carboxylic-acid.
BibTeX @misc{4ortxyz_1-3-4-trihydroxy-5-3-4-5-trihydroxybenzoyl-oxycyclohexane-1-carboxylic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid}}, year = {2026}, url = {https://4ort.xyz/entity/1-3-4-trihydroxy-5-3-4-5-trihydroxybenzoyl-oxycyclohexane-1-carboxylic-acid}, note = {Accessed: 2026-05-03}}
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